Table 3:

Kits based on ‘not identified’ mechanism

Authorization	Manufacturer	Mechanism	Target	LOD	Time
-	Biological Technologies Co., LTD	-	-	-	-
-	(Chongqing) Bio-tech, Co., Ltd	-	-	-	-
-	Health Technology Co., Ltd	-	-	-	-
-	Bio-tech Co., Ltd	-	-	-	-
-	Medical Technology Co., Ltd	-	-	-	-
-	Biotechnologies (Hangzhou) Ltd	-	-	-	-
-	Biomedicine Co., Ltd.	-	-	-	-

^*US EUA Authorized,

^**US EUA Planned,

^***US Notified FDA under section IV.D,

^****US EUA Submitted,

^#European Union Conformity Marked,

^$The National Medical Product Administration Authorized China,

^$$Korea Ministry of Food and Drug Safety,

^$$$Philippines Food and Drug Administration,

^€Singapore Health Sciences Authority, personal authorization for clinical use,

^ƛEUA India,

^ψKorea Centers for Disease Control and the Korea Food and Drug Administration

^-Data Not Available

References for kits in table 1–3:

https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/vitro-diagnostics-euas

http://ph.china-embassy.org/eng/sgdt/t1760281.htm.

https://www.modernhealthcare.com/safety/coronavirus-test-tracker-commercially-available-covid-19-diagnostic-tests.

https://www.finddx.org/covid-19/pipeline/.